T39P (p.Thr39Pro) variant of F10 (Coagulation factor X)
T39P (p.Thr39Pro) in F10 (Coagulation factor X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
T39P (p.Thr39Pro) variant details
- p.Thr39Pro
- 1000Genomes rs188917950
- ExAC rs188917950
- TOPMed rs188917950
- gnomAD rs188917950
- Missense
- Variant Prioritization Score for Impact Estimate 0.296
- REVEL 0.27
- CADD 14.30
- PolyPhen-2 0.00
- SIFT 0.01
- Most common in the 1KG:JPT population (allele frequency 0.0049)
- Structural context available